Resumen
Rationale: The epidemiology and prognostic impact of increased pulmonary pressure among HIV-infected individuals in the antiretroviral therapy era is not well described. Objectives: To examine the prevalence, clinical features, and outcomes of increased echocardiographic pulmonary pressure in HIV-infected and -uninfected individuals. Methods: This study evaluated 8,296 veterans referred for echocardiography with reported pulmonary artery systolic pressure (PASP) estimates from the Veterans Aging Cohort study, an observational cohort of HIV-infected and -uninfected veterans matched by age, sex, race/ethnicity, and clinical site. The primary outcome was adjusted mortality by HIV status. MeasurementsandMainResults:PASPwas reported in2,831HIVinfectedand5,465HIV- uninfectedveterans (follow-up[mean ± SD], 3.8 ± 2.6 yr). As compared with uninfected veterans, HIV-infected veterans with HIV viral load greater than 500 copies/ml (odds ratio, 1.27; 95%confidence interval [CI], 1.05-1.54) and those withCD4 cell count less than 200 cells/ml (odds ratio, 1.28; 95%CI, 1.02-1.60) had a higher prevalence ofPASPgreater than or equal to 40 mm Hg. As compared with uninfected veterans with a PASP less than 40mmHg,HIV-infected veteranswith a PASP greater than or equal to 40mmHg had an increased risk of death (adjusted hazard ratio, 1.78;95%CI, 1.57-2.01).This riskpersisted evenamongparticipants without prevalent comorbidities (adjusted hazard ratio, 3.61;95%CI, 2.17-6.01).The adjusted risk of mortality in HIV-infected veterans was higher at all PASP valuesthan inuninfectedveterans, includingat values currentlyconsidered to be normal. Conclusions: HIV-infected people with high HIV viral loads or low CD4 cell counts have a higher prevalence of increased PASP than uninfected people. Mortality risk in HIV-infected veterans increases at lower values of PASP than previously recognized and is present even among those without prevalent comorbidities. These findings may inform clinical decision-making regarding screening and surveillance of pulmonary hypertension in HIV-infected individuals.
| Idioma original | English |
|---|---|
| Páginas (desde-hasta) | 923-932 |
| Número de páginas | 10 |
| Publicación | American Journal of Respiratory and Critical Care Medicine |
| Volumen | 197 |
| N.º | 7 |
| DOI | |
| Estado | Published - abr 1 2018 |
Nota bibliográfica
Publisher Copyright:Copyright © 2018 by the American Thoracic Society.
Financiación
Supported by American Heart Association Fellow to Faculty Grant 13FTF16070002 (E.L.B.), Gilead Sciences Scholars Program in Pulmonary Arterial Hypertension (E.L.B.), and grants U24AA020794 (A.J.) and U01AA020790 (A.J.) from the National Institute on Alcohol Abuse and Alcoholism, and R01HL25032 from the NHLBI (M.F.). Support for Veterans Affairs/Centers for Medicare and Medicaid Services data is provided by the Department of Veterans Affairs, Veterans Health Administration, Office of Research and Development, Health Services Research and Development, and Veterans Affairs Information Resource Center (project numbers SDR 02-237 and 98-004).
| Financiadores | Número del financiador |
|---|---|
| National Institute on Alcohol Abuse and Alcoholism | U24AA020794, U01AA020790, R01HL25032 |
| National Institute on Alcohol Abuse and Alcoholism | |
| National Heart, Lung, and Blood Institute (NHLBI) | |
| American the American Heart Association | 13FTF16070002 |
| American the American Heart Association | |
| Gilead Sciences | |
| Biomedical Laboratory Research and Development, VA Office of Research and Development |
ODS de las Naciones Unidas
Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible
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Good health and well being
ASJC Scopus subject areas
- Pulmonary and Respiratory Medicine
- Critical Care and Intensive Care Medicine
Huella
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